rs113488022, BRAF

N. diseases: 490
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Adenoma, Villous
CUI: C0206674
Disease: Adenoma, Villous
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Prostatic Neoplasms
CUI: C0033578
Disease: Prostatic Neoplasms
31 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Gastrointestinal Carcinoid Tumor
CUI: C0220620
Disease: Gastrointestinal Carcinoid Tumor
13 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2009 2009
Hypocholesterolemia
CUI: C0151718
Disease: Hypocholesterolemia
22 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2009 2009
Thyroid cancer, follicular
CUI: C2931367
Disease: Thyroid cancer, follicular
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2007 2010
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1 2010 2010
Eruptive melanocytic nevi
CUI: C1304321
Disease: Eruptive melanocytic nevi
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2010 2010
Juvenile Pilocytic Astrocytoma
CUI: C0280783
Disease: Juvenile Pilocytic Astrocytoma
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2010 2010
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2008 2011
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
82 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.710 1.000 1 2011 2011
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
Congenital melanocytic nevus
CUI: C1318558
Disease: Congenital melanocytic nevus
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
Congenital Mesoblastic Nephroma
CUI: C1332965
Disease: Congenital Mesoblastic Nephroma
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
Marinesco-Sjogren syndrome
CUI: C0024814
Disease: Marinesco-Sjogren syndrome
8 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2011 2011
Clear Cell Sarcoma of Soft Tissue
CUI: C0206651
Disease: Clear Cell Sarcoma of Soft Tissue
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2005 2012
Familial Nonmedullary Thyroid Gland Carcinoma
CUI: C3896673
Disease: Familial Nonmedullary Thyroid Gland Carcinoma
6 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2005 2012
Stage III Colon Cancer
CUI: C0278480
Disease: Stage III Colon Cancer
3 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2010 2012
Stage III Colon Cancer AJCC v7
CUI: C3146254
Disease: Stage III Colon Cancer AJCC v7
3 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2010 2012
Stage III Colon Cancer AJCC v8
CUI: C4525124
Disease: Stage III Colon Cancer AJCC v8
3 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.020 1.000 2 2010 2012
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012
Arthralgia
CUI: C0003862
Disease: Arthralgia
27 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2012 2012